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foretinib
Known as:
N-(3-Fluoro-4-((6-methoxy-7-(3-(morpholin-4-yl)propoxy)quinolin-4-yl)oxy)phenyl)-N'-(4-fluorophenyl)cyclopropane-1,1-dicarboxamide
An orally bioavailable small molecule with potential antineoplastic activity. Foretinib binds to and selectively inhibits hepatocyte growth factor…
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National Institutes of Health
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Related topics
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4 relations
Broader (1)
GSK 1363089
NCIt Antineoplastic Agent Terminology
Receptor Tyrosine Kinase Inhibition
XL880
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2020
2020
Design, synthesis and biological evaluation of novel N-sulfonylamidine-based derivatives as c-Met inhibitors via Cu-catalyzed three-component reaction.
Xiang Nan
,
Jing Zhang
,
+4 authors
Yanchao Wu
European journal of medicinal chemistry
2020
Corpus ID: 219452459
2019
2019
Design, synthesis and evaluation of sulfonylurea-containing 4-phenoxyquinolines as highly selective c-Met kinase inhibitors.
Xiang Nan
,
Yihan Jiang
,
Hui-Jing Li
,
Jun-Hu Wang
,
Yanchao Wu
Bioorganic & Medicinal Chemistry
2019
Corpus ID: 153306867
2018
2018
Foretinib Overcomes Entrectinib Resistance Associated with the NTRK1 G667C Mutation in NTRK1 Fusion–Positive Tumor Cells in a Brain Metastasis Model
A. Nishiyama
,
Tadaaki Yamada
,
+10 authors
S. Yano
Clinical Cancer Research
2018
Corpus ID: 4580597
Purpose: Rearrangement of the neurotrophic tropomyosin receptor kinase 1 (NTRK1) gene, which encodes tyrosine receptor kinase A…
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2018
2018
Design, Synthesis and Biological Evaluation of 6,7-Disubstituted-4-phenoxyquinoline Derivatives Bearing Pyridazinone Moiety as c-Met Inhibitors
Xiaobo Liu
,
Jianlan Kou
,
+4 authors
Wufu Zhu
Molecules
2018
Corpus ID: 49479645
Deregulation of the receptor tyrosine kinase mesenchymal epithelial transition factor (MET) has been implicated in several human…
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2016
2016
Cabozantinib in Advanced Renal Cell Carcinoma: Is it a METEOR?
C. Ciccarese
,
F. Massari
,
G. Tortora
European Urology
2016
Corpus ID: 3416305
2014
2014
Design, synthesis and biological evaluation of novel 6,7-disubstituted-4-phenoxyquinoline derivatives bearing 4-oxo-3,4-dihydrophthalazine-1-carboxamide moieties as c-Met kinase inhibitors.
Zijian Liu
,
Rui Wang
,
+4 authors
P. Gong
Bioorganic & Medicinal Chemistry
2014
Corpus ID: 34492981
2013
2013
Erratum to: A Phase 1 dose-escalation study of the safety and pharmacokinetics of once-daily oral foretinib, a multi-kinase inhibitor, in patients with solid tumors
G. Shapiro
,
S. McCallum
,
+10 authors
P. LoRusso
Investigational new drugs
2013
Corpus ID: 39479891
Foretinib is an oral multi-kinase inhibitor targeting MET, vascular endothelial growth factor receptor (VEGFR)-2, RON, KIT, and…
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2012
2012
A Comparison of the pharmacokinetics of the anticancer MET inhibitor foretinib free base tablet formulation to bisphosphate salt capsule formulation in patients with solid tumors
A. Naing
,
R. Kurzrock
,
+7 authors
P. LoRusso
Investigational new drugs
2012
Corpus ID: 2998824
SummaryPurpose This phase I, open-label, randomized, 2-part crossover study assessed the safety, pharmacokinetics and relative…
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Review
2012
Review
2012
A phase II study of foretinib in triple-negative, recurrent/metastatic breast cancer: NCIC CTG trial IND.197 (NCT01147484).
D. Rayson
,
S. Lupichuk
,
+13 authors
E. Eisenhauer
2012
Corpus ID: 59215204
1036 Background: Met, a receptor tyrosine kinase, is preferentially expressed in basal-like compared to luminal breast cancer. In…
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2011
2011
Mechanism of action of the multikinase inhibitor Foretinib
M. Dufies
,
A. Jacquel
,
+8 authors
P. Auberger
Cell Cycle
2011
Corpus ID: 29250726
Mitotic catastrophe (MC) is induced when stressed cells enter prematurely or inappropriately into mitosis and can be caused by…
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